G37G (p.Gly37Gly) variant of SDHAF2 (Q9NX18)
G37G (p.Gly37Gly) in SDHAF2 (Q9NX18) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.21 / 1. The record also includes population frequency data, published literature, and structural context.
G37G (p.Gly37Gly) variant details
- p.Gly37Gly
- gnomAD 11-61437699-T-G
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.206
- CADD 9.62
- Most common in the Non-Finnish European population (allele frequency 9e-07)
- Structural context available
- Literature evidence available